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123994-80-9

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123994-80-9 Usage

Chemical compound

2-[(3,4-difluorophenyl)amino]-3,7-dihydro-6H-purin-6-one

Class

Purine analogues

Mechanism of action

Non-nucleoside inhibitor of the viral RNA-dependent RNA polymerase

Potential use

Treatment for hepatitis C

Mode of action

Interferes with replication of hepatitis C virus

Suitability

Promising candidate for combination therapies for hepatitis C

Clinical trials

Subject of several trials with efficacy in reducing viral load

Approval status

Not yet approved for commercial use

Promise

Potential treatment option for hepatitis C infection

Check Digit Verification of cas no

The CAS Registry Mumber 123994-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,9 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123994-80:
(8*1)+(7*2)+(6*3)+(5*9)+(4*9)+(3*4)+(2*8)+(1*0)=149
149 % 10 = 9
So 123994-80-9 is a valid CAS Registry Number.

123994-80-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-difluoroanilino)-3,7-dihydropurin-6-one

1.2 Other means of identification

Product number -
Other names 6H-Purin-6-one,2-[(3,4-difluorophenyl)amino]-1,9-dihydro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:123994-80-9 SDS

123994-80-9Downstream Products

123994-80-9Relevant articles and documents

Structure-Activity Relationships of N2-Substituted Guanines as Inhibitors of HSV1 and HSV2 Thymidine Kinases

Hildebrand, Catherine,Sandoli, Daniele,Focher, Federico,Gambino, Joseph,Ciarrocchi, Giovanni,et al.

, p. 203 - 206 (2007/10/02)

A series of N2-phenylguanines was synthesized and tested for inhibition of the thymidine kinases encoded by Herpes simplex viruses type 1 and type 2.Compounds with hydrophobic, electron-attracting groups in the meta position of the phenyl ring

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